UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000001540 |
|---|---|
| Receipt number | R000001864 |
| Scientific Title | A Phase I Dose Intensification Study of three dimentional conformal thoracic radiotherapy with concurrent cisplatin and TS-1 for unresectable stage III non-small cell lung cancer |
| Date of disclosure of the study information | 2008/12/02 |
| Last modified on | 2013/06/03 11:13:32 |
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Basic information
Public title
A Phase I Dose Intensification Study of three dimentional conformal thoracic radiotherapy with concurrent cisplatin and TS-1 for unresectable stage III non-small cell lung cancer
Acronym
Dose intensification study of 3DCRT concurrent with CDDP and S1 for stage III NSCLC.
Scientific Title
A Phase I Dose Intensification Study of three dimentional conformal thoracic radiotherapy with concurrent cisplatin and TS-1 for unresectable stage III non-small cell lung cancer
Scientific Title:Acronym
Dose intensification study of 3DCRT concurrent with CDDP and S1 for stage III NSCLC.
Region
| Japan |
Condition
Condition
non-small cell lung cancer
Classification by specialty
| Medicine in general | Pneumology | Hematology and clinical oncology |
| Radiology |
Classification by malignancy
Malignancy
Genomic information
NO
Objectives
Narrative objectives1
To determin Maximum Torelated Dose and Recommended dose of thoracic radiotherapy for stage III NSCLC.
Basic objectives2
Efficacy
Basic objectives -Others
Trial characteristics_1
Exploratory
Trial characteristics_2
Pragmatic
Developmental phase
Phase I,II
Assessment
Primary outcomes
To determin Maximum Torelated Dose and Recommended dose of thoracic radiotherapy for stage III NSCLC.
Key secondary outcomes
Toxicity, Response rate, Survival
Base
Study type
Interventional
Study design
Basic design
Single arm
Randomization
Non-randomized
Randomization unit
Blinding
Open -no one is blinded
Control
Uncontrolled
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment
Intervention
No. of arms
1
Purpose of intervention
Treatment
Type of intervention
| Medicine | Device,equipment |
Interventions/Control_1
Chemo-Radiotherapy
Interventions/Control_2
Interventions/Control_3
Interventions/Control_4
Interventions/Control_5
Interventions/Control_6
Interventions/Control_7
Interventions/Control_8
Interventions/Control_9
Interventions/Control_10
Eligibility
Age-lower limit
| 20 | years-old | <= |
Age-upper limit
| 75 | years-old | >= |
Gender
Male and Female
Key inclusion criteria
StageIIIA,orIIIB NSCLC.
No previous treatment
Measurable lesion
20 - 75years old.
Performance status 0-1
Adequate organ functionWritten
informed consent
Key exclusion criteria
Interstitial pneumonia.
No eligibility for definitive radiotherapy.
Target sample size
27
Research contact person
Name of lead principal investigator
| 1st name | |
| Middle name | |
| Last name | Hideyuki Harada |
Organization
Shizuoka Cancer Center
Division name
Radiation Oncology
Zip code
Address
Shimonagakubo 1007, Nagaizumi-cho, Sunto-Gun, Shizuoka, Japan
TEL
Public contact
Name of contact person
| 1st name | |
| Middle name | |
| Last name |
Organization
Shizuoka Cancer Center
Division name
Radiation Oncology
Zip code
Address
TEL
Homepage URL
h.harada@scchr.jp
Sponsor or person
Institute
Shizuoka Cancer Center, The Cancer Institute Hospital of JFCR
Institute
Department
Personal name
Funding Source
Organization
None
Organization
Division
Category of Funding Organization
Self funding
Nationality of Funding Organization
Other related organizations
Co-sponsor
Name of secondary funder(s)
IRB Contact (For public release)
Organization
Address
Tel
Secondary IDs
Secondary IDs
NO
Study ID_1
Org. issuing International ID_1
Study ID_2
Org. issuing International ID_2
IND to MHLW
Institutions
Institutions
Other administrative information
Date of disclosure of the study information
| 2008 | Year | 12 | Month | 02 | Day |
Related information
URL releasing protocol
Publication of results
Published
Result
URL related to results and publications
Number of participants that the trial has enrolled
Results
The radiation dose of 74Gy in 37 frs with CDDP+S-1 seemed to be torelable.
Results date posted
Results Delayed
Results Delay Reason
Date of the first journal publication of results
Baseline Characteristics
Participant flow
Adverse events
Outcome measures
Plan to share IPD
IPD sharing Plan description
Progress
Recruitment status
Completed
Date of protocol fixation
| 2007 | Year | 08 | Month | 21 | Day |
Date of IRB
Anticipated trial start date
| 2007 | Year | 09 | Month | 01 | Day |
Last follow-up date
| 2011 | Year | 03 | Month | 01 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
Management information
Registered date
| 2008 | Year | 12 | Month | 02 | Day |
Last modified on
| 2013 | Year | 06 | Month | 03 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000001864
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| Registered date | File name |
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